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corneal dystrophy

Go to external page http://purl.obolibrary.org/obo/MONDO_0018102

The term corneal dystrophy embraces a heterogeneous group of bilateral genetically determined non-inflammatory corneal diseases that are usually restricted to the cornea. The designation is imprecise but remains in vogue because of its clinical value. [ Orphanet:34533 ]

Synonyms: corneal dystrophy (disease) corneal dystrophy

This is just here as a test because I lose it

Term information

database cross reference
  • MEDGEN:3619 (MONDO:equivalentTo)
  • MESH:D003317 (Orphanet:34533/e)
  • SCTID:5587004 (MONDO:equivalentTo)
  • Orphanet:34533 (MONDO:equivalentTo)
  • icd11.foundation:1291475891 (https://orcid.org/0000-0001-5208-3432)
  • UMLS:C0010036 (MONDO:equivalentTo)
  • DOID:2566 (MONDO:equivalentTo)
  • MedDRA:10011005 (Orphanet:34533/e)
  • ICD9:371.50 (DOID:2566)
  • ICD9:371.5 (DOID:2566)
  • HP:0001131 (MONDO:otherHierarchy)
  • NCIT:C34513 (MONDO:equivalentTo)
Subsets

otar, disease_grouping, rare, nord_rare, ordo_group_of_disorders

IAO 0000589

corneal dystrophy (disease)

closeMatch

http://identifiers.org/meddra/10011005

comment

Editor note: NCIT distinguishes between acquired and genetic

exactMatch

http://purl.obolibrary.org/obo/DOID_2566

http://purl.obolibrary.org/obo/NCIT_C34513

http://www.orpha.net/ORDO/Orphanet_34533

http://identifiers.org/snomedct/5587004

http://identifiers.org/medgen/3619

http://linkedlifedata.com/resource/umls/id/C0010036

http://identifiers.org/mesh/D003317

id

MONDO:0018102

Term relations

Subclass of: